DOP2018000065A - DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENT - Google Patents

DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENT

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Publication number
DOP2018000065A
DOP2018000065A DO2018000065A DO2018000065A DOP2018000065A DO P2018000065 A DOP2018000065 A DO P2018000065A DO 2018000065 A DO2018000065 A DO 2018000065A DO 2018000065 A DO2018000065 A DO 2018000065A DO P2018000065 A DOP2018000065 A DO P2018000065A
Authority
DO
Dominican Republic
Prior art keywords
quinolin
atm
isopropilimidazo
propoxi
piridil
Prior art date
Application number
DO2018000065A
Other languages
Spanish (es)
Inventor
Gordon Pike Kurt
Anthony Hunt Thomas
John Eatherton Andrew
Chistophe Barlaam Bernard
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of DOP2018000065A publication Critical patent/DOP2018000065A/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La memoria descriptiva se refiere en general a compuestos de Fórmula (I): (I) y sales farmacéuticamente aceptables de estos, donde R1, R2, R3, R4 y R5 tienen cualquiera de los significados definidos en la presente. La memoria descriptiva también se refiere al uso de compuestos de Fórmula (I) y sales de estos para tratar o prevenir una enfermedad mediada por ATM, incluido el cáncer. La memoria descriptiva se refiere además a composiciones farmacéuticas que comprenden compuestos de tipo imidazo[4,5-c]quinolin-2-ona sustituidos y sales farmacéuticamente aceptables de estos; kits que comprenden tales compuestos y sales; métodos de producción de tales compuestos y sales; e intermedios útiles en tal producción.The specification refers in general to compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, where R1, R2, R3, R4 and R5 have any of the meanings defined herein. The specification also refers to the use of compounds of Formula (I) and salts thereof to treat or prevent an ATM-mediated disease, including cancer. The specification also relates to pharmaceutical compositions comprising imidazo [4,5-c] quinolin-2-one substituted compounds and pharmaceutically acceptable salts thereof; kits comprising such compounds and salts; production methods of such compounds and salts; and intermediates useful in such production.

DO2018000065A 2015-09-17 2018-03-06 DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENT DOP2018000065A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB1516504.6A GB201516504D0 (en) 2015-09-17 2015-09-17 Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer

Publications (1)

Publication Number Publication Date
DOP2018000065A true DOP2018000065A (en) 2018-03-30

Family

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Family Applications (1)

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DO2018000065A DOP2018000065A (en) 2015-09-17 2018-03-06 DERIVATIVES OF 8- [6- [3- (AMINO) PROPOXI] -3-PIRIDIL] 1-ISOPROPILIMIDAZO [4,5-C] QUINOLIN-2-ONA AS SELECTED MODULATORS OF THE MUTED TELANGIECTASIA ATAXIA KINASE (ATM) FOR THE CANCER TREATMENT

Country Status (37)

Country Link
US (5) US9856255B2 (en)
EP (2) EP3683220B1 (en)
JP (1) JP6605130B2 (en)
KR (2) KR102469153B1 (en)
CN (1) CN108137576B (en)
AR (1) AR106053A1 (en)
AU (1) AU2016323399B2 (en)
BR (1) BR112018004325B1 (en)
CA (1) CA2997399C (en)
CL (1) CL2018000677A1 (en)
CO (1) CO2018002829A2 (en)
CR (1) CR20180172A (en)
CY (1) CY1124680T1 (en)
DK (2) DK3683220T3 (en)
DO (1) DOP2018000065A (en)
EA (1) EA033284B1 (en)
ES (2) ES2853924T3 (en)
GB (1) GB201516504D0 (en)
HK (2) HK1255408A1 (en)
HR (1) HRP20210149T1 (en)
HU (2) HUE053066T2 (en)
IL (1) IL257847B (en)
LT (1) LT3350180T (en)
MX (1) MX2018003186A (en)
MY (1) MY195669A (en)
NI (1) NI201800033A (en)
PE (1) PE20181078A1 (en)
PH (1) PH12018500532A1 (en)
PL (2) PL3350180T3 (en)
PT (2) PT3683220T (en)
RS (1) RS61435B1 (en)
SI (1) SI3350180T1 (en)
SV (1) SV2018005655A (en)
TN (1) TN2018000078A1 (en)
TW (2) TWI714631B (en)
WO (1) WO2017046216A1 (en)
ZA (1) ZA202209171B (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201516504D0 (en) * 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
GB201608227D0 (en) * 2016-05-11 2016-06-22 Astrazeneca Ab Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer
JOP20190209A1 (en) * 2017-03-16 2019-09-12 Astrazeneca Ab Deuterated imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer
CN111344293A (en) 2017-09-20 2020-06-26 阿斯利康(瑞典)有限公司 1, 3-dihydroimidazo [4, 5-c ] cinnolin-2-one compounds and their use in the treatment of cancer
WO2020052688A1 (en) 2018-09-14 2020-03-19 Suzhou Zanrong Pharma Limited 1-ISOPROPYL-3-METHYL-8- (PYRIDIN-3-YL) -1, 3-DIHYDRO-2H-IMIDAZO [4, 5-c] CINNOLIN-2-ONE AS SELECTIVE MODULATORS OF ATAXIA TELANGIECTASIA MUTATED (ATM) KINASE AND USES THEREOF
WO2021139814A1 (en) * 2020-01-09 2021-07-15 南京明德新药研发有限公司 Quinoline imidazole compound and application thereof
US20230293507A1 (en) * 2020-03-04 2023-09-21 Pharos Ibio Co., Ltd Use of 2,3,5-substituted thiophene compound for preventing, ameliorating, or treating ovarian cancer
JP2023539715A (en) 2020-06-24 2023-09-19 アストラゼネカ ユーケー リミテッド Combination of antibody-drug conjugates and ATM inhibitors
EP4219499A1 (en) * 2020-09-28 2023-08-02 CSPC Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd. A class of fused ring compounds, and preparation and use thereof
EP3992191A1 (en) 2020-11-03 2022-05-04 Deutsches Krebsforschungszentrum Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors
WO2022125614A1 (en) * 2020-12-09 2022-06-16 Stingray Therapeutics, Inc. Phosphonates as inhibitors of enpp1 and cdnp
AU2021433713A1 (en) * 2021-03-17 2023-09-28 Suzhou Zanrong Pharma Limited Selective modulators of ataxia telangiectasia mutated (atm) kinase and uses thereof
CN115304598B (en) * 2021-08-25 2024-05-31 石药集团中奇制药技术(石家庄)有限公司 Heterocyclic compound, and preparation method and application thereof
GB202114704D0 (en) 2021-10-14 2021-12-01 Univ Birmingham ATM inhibition
IL314381A (en) * 2022-01-26 2024-09-01 Chia Tai Tianqing Pharmaceutical Group Co Ltd Hydrazino group-containing compound
WO2023200427A1 (en) * 2022-04-11 2023-10-19 Wei Zhong Substituted 1-(3,3-difluoropiperidin-4-yl)-imidazo[4,5-c] quinolin-2-one derivative crystal form, salt crystal form, preparation method and application

Family Cites Families (92)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ240313A (en) 1990-10-22 1994-04-27 Res Corp Technologies Inc Anti-retrovirus compositions containing aryl and heteroaryl derivatives
TW301607B (en) 1993-03-09 1997-04-01 Takeda Pharm Industry Co Ltd
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
KR19990082463A (en) 1996-02-13 1999-11-25 돈 리사 로얄 Quinazolin derivatives as vascular endothelial growth factor inhibitors
CN1116286C (en) 1996-03-05 2003-07-30 曾尼卡有限公司 4-anilinoquinazoline derivatives
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
US6632823B1 (en) 1997-12-22 2003-10-14 Merck & Co., Inc. Substituted pyridine compounds useful as modulators of acetylcholine receptors
JP2002522388A (en) 1998-08-03 2002-07-23 ビーエーエスエフ コーポレーション Pyridinone for the treatment of sexual dysfunction
EP1150955A2 (en) 1999-02-04 2001-11-07 Millennium Pharmaceuticals, Inc. G-protein coupled heptahelical receptor binding compounds and methods of use thereof
US20020151712A1 (en) 1999-09-14 2002-10-17 Nan-Horng Lin 3-pyrrolidinyloxy-3'-pyridyl ether compounds useful for controlling chemical synaptic transmission
WO2002030357A2 (en) 2000-10-11 2002-04-18 Chemocentryx, Inc. Compounds and methods for modulating ccr4 function
AU2002213467A1 (en) 2000-10-11 2002-04-22 Chemocentryx, Inc. Modulation of ccr4 function
EP1217000A1 (en) 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibitors of factor Xa and factor VIIa
WO2002076177A2 (en) 2001-03-23 2002-10-03 Bethesda Pharmaceuticals, Inc. Design and synthesis of optimized ligands for ppar
JP2002293745A (en) 2001-03-29 2002-10-09 St Marianna Univ School Of Medicine Therapeutic agent for chronic rheumatism
CA2442654A1 (en) 2001-04-10 2002-10-10 Transtech Pharma, Inc. Probes, systems, and methods for drug discovery
WO2002087618A1 (en) 2001-04-27 2002-11-07 Takeda Chemical Industries, Ltd. Preventive/therapeutic method for cancer
WO2002094264A1 (en) 2001-05-23 2002-11-28 Tularik Inc. Ccr4 antagonists
EP1270535A3 (en) 2001-06-20 2004-02-18 Clariant GmbH Method to synthesise substituted aromatic compounds
JP4082888B2 (en) 2001-10-17 2008-04-30 広栄化学工業株式会社 Process for producing biaryl compounds
WO2003062392A2 (en) 2002-01-18 2003-07-31 Ceretek Llc Methods of treating conditions associated with an edg receptor
JP4167848B2 (en) 2002-04-10 2008-10-22 広栄化学工業株式会社 Process for producing biaryl compounds
GB0211649D0 (en) 2002-05-21 2002-07-03 Novartis Ag Organic compounds
US20060004010A1 (en) 2002-07-10 2006-01-05 Hiromu Habashita Ccr4 antagonist and medical use thereof
CN1678303A (en) 2002-08-23 2005-10-05 康涅狄格大学 Keto cannabinoids with therapeutic indications
US20040087590A1 (en) 2002-08-23 2004-05-06 University Of Connecticut Novel biphenyl and biphenyl-like cannabinoids
EP1599475A2 (en) 2003-03-06 2005-11-30 Eisai Co., Ltd. Jnk inhibitors
WO2004080943A1 (en) 2003-03-11 2004-09-23 Ono Pharmaceutical Co., Ltd. Cinnamyl alcohol derivative compounds and drugs containing the compounds as the active ingredient
WO2004113258A1 (en) 2003-06-20 2004-12-29 Shionogi & Co., Ltd. Carbon-carbon bond forming reaction
JPWO2005023771A1 (en) 2003-09-05 2006-11-02 小野薬品工業株式会社 Chemokine receptor antagonist and its pharmaceutical use
JP2005170939A (en) 2003-11-20 2005-06-30 Takeda Chem Ind Ltd Prophylactic/therapeutic agent for diabetes
KR20060117329A (en) 2003-11-21 2006-11-16 노파르티스 아게 1h-imidazoquinoline derivatives as protein kinase inhibitors
WO2006038594A1 (en) 2004-10-04 2006-04-13 Ono Pharmaceutical Co., Ltd. N-type calcium channel inhibitor
JP4318087B2 (en) 2004-12-13 2009-08-19 小野薬品工業株式会社 Aminocarboxylic acid derivatives and their pharmaceutical use
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
US20070032522A1 (en) 2005-07-01 2007-02-08 Kumar Dange V Antiviral agents
EP1962861A2 (en) 2005-08-26 2008-09-03 Emory University Compounds and methods for modulating the silencing of a polynucleotide of interest
JO3598B1 (en) 2006-10-10 2020-07-05 Infinity Discovery Inc Boronic acids and esters as inhibitors of fatty acid amide hydrolase
JP2009023986A (en) 2006-11-08 2009-02-05 Pharma Ip Biaryl derivative as anticancer agent
CL2008000191A1 (en) 2007-01-25 2008-08-22 Astrazeneca Ab COMPOUNDS DERIVED FROM 4-AMINO-CINNOTINA-3-CARBOXAMIDA; CSF-1R QUINASA INHIBITORS; YOUR PREPARATION PROCESS; AND ITS USE TO TREAT CANCER.
US9370508B2 (en) 2007-02-20 2016-06-21 Novartis Ag Imidazoquinolines as dual lipid kinase and mTOR inhibitors
JP2010520293A (en) 2007-03-07 2010-06-10 アラントス・フアーマシユーテイカルズ・ホールデイング・インコーポレイテツド Metalloprotease inhibitors containing heterocyclic moieties
US8039505B2 (en) 2007-04-11 2011-10-18 University Of Utah Research Foundation Compounds for modulating T-cells
PE20090717A1 (en) 2007-05-18 2009-07-18 Smithkline Beecham Corp QUINOLINE DERIVATIVES AS PI3 KINASE INHIBITORS
US7928111B2 (en) 2007-06-08 2011-04-19 Senomyx, Inc. Compounds including substituted thienopyrimidinone derivatives as ligands for modulating chemosensory receptors
US9321730B2 (en) 2007-08-21 2016-04-26 The Hong Kong Polytechnic University Method of making and administering quinoline derivatives as anti-cancer agents
CN101980708B (en) 2008-03-26 2013-03-13 诺瓦提斯公司 Imidazoquinolines and pyrimidine derivatives as potent modulators of VEGF-driven angiogenic processes
AU2009266956B2 (en) 2008-07-01 2014-03-20 Genentech, Inc. Bicyclic heterocycles as MEK kinase inhibitors
TW201028381A (en) 2008-07-14 2010-08-01 Shionogi & Co Pyridine derivative having ttk inhibition activity
US8791131B2 (en) 2008-09-30 2014-07-29 Pfizer Inc. Imidazo[1,5]naphthyridine compounds, their pharmaceutical use and compositions
WO2010077680A2 (en) 2008-12-08 2010-07-08 Vm Discovery Inc. Compositions of protein receptor tyrosine kinase inhibitors
US20120093917A1 (en) 2009-04-02 2012-04-19 Robert Hromas Metnase and intnase inhibitors and their use in treating cancer
TW201041888A (en) 2009-05-06 2010-12-01 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
MX2011012943A (en) * 2009-06-04 2012-01-27 Novartis Ag 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES.
WO2010139747A1 (en) * 2009-06-04 2010-12-09 Novartis Ag 1H-IMIDAZO[4, 5-c]QUINOLINONE COMPOUNDS, USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES
JP5546636B2 (en) 2009-09-28 2014-07-09 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト Benzoxepin PI3K inhibitor compounds and methods of use
GB0919423D0 (en) 2009-11-05 2009-12-23 Glaxosmithkline Llc Novel compounds
CN102199152A (en) 2010-03-25 2011-09-28 高大新 Heterocycle imidazoles phosphatide kinases inhibitor
CN102372711B (en) * 2010-08-18 2014-09-17 山东轩竹医药科技有限公司 Imidazo quinoline PI3K and mTOR (mammalian target of rapamycin) dual inhibitor
US20120046272A1 (en) 2010-08-23 2012-02-23 Grunenthal Gmbh Novel Therapeutic Compounds
DE102010035744A1 (en) * 2010-08-28 2012-03-01 Merck Patent Gmbh Imidazolonylchinoline
CN102399218A (en) * 2010-09-16 2012-04-04 和记黄埔医药(上海)有限公司 Triheterocyclic compounds and their use as PI3K inhibitors
AR083267A1 (en) 2010-10-04 2013-02-13 Novartis Ag PHARMACEUTICAL COMBINATIONS
MA34806B1 (en) 2010-12-03 2014-01-02 Novartis Ag PHARMACEUTICAL COMPOSITIONS
AU2011340167A1 (en) 2010-12-06 2013-07-18 Piramal Enterprises Limited Substituted imidazoquinoline derivatives
WO2012083866A1 (en) 2010-12-22 2012-06-28 The Hong Kong Polytechnic University Quinoline derivatives as anti-cancer agents
TWI450891B (en) 2010-12-29 2014-09-01 Dev Center Biotechnology Novel tubulin inhibitors
JO3003B1 (en) * 2011-01-14 2016-09-05 Lilly Co Eli Imidazo [4,5-c] quinolin-2-one compound and its use as pi3 kinase i mtor dual inhibitor
EP2694678A2 (en) 2011-04-04 2014-02-12 Netherland Cancer Institute Methods and compositions for predicting resistance to anticancer treatment
US9884828B2 (en) 2011-05-23 2018-02-06 Imago Pharmaceuticals, Inc. Substituted cinnolines as inhibitors of LRRK2 kinase activity
US10533000B2 (en) 2011-05-26 2020-01-14 Sunovion Pharmaceuticals, Inc. Metabotrophic glutamate receptor 5 modulators and methods of use thereof
WO2013022740A2 (en) 2011-08-05 2013-02-14 Corning Incorporated Gpr35 ligands and the uses thereof
JP6042060B2 (en) 2011-09-26 2016-12-14 サノフイ Pyrazoloquinolinone derivatives, their preparation and therapeutic use
EP2776437B1 (en) 2011-11-07 2018-09-26 Sunovion Pharmaceuticals Inc. Modulators of opioid receptors and methods of use thereof
WO2013074965A1 (en) 2011-11-16 2013-05-23 Microbiotix, Inc. Aminoalkyl phenol ether inhibitors of influenza a virus
WO2013157018A1 (en) 2012-04-18 2013-10-24 Indian Institute Of Technology Madras A process for the preparation of the core structure in quinolone and napthyridone class of antibiotics
CA2872541A1 (en) 2012-06-06 2013-12-12 Novartis Ag Combination of a 17 -alpha -hydroxylase (c17, 20 - lyase) inhibitor and a specific pi-3k inhibitor for treating a tumor disease
AU2013271731A1 (en) 2012-06-07 2014-12-18 Georgia State University Research Foundation, Inc. SecA inhibitors and methods of making and using thereof
WO2013192367A1 (en) 2012-06-22 2013-12-27 Novartis Ag Neuroendocrine tumor treatment
MX369518B (en) 2012-08-16 2019-11-11 Novartis Ag Combination of pi3k inhibitor and c-met inhibitor.
WO2014031872A2 (en) 2012-08-23 2014-02-27 The Broad Institute, Inc. Small molecule inhibitors for treating parasitic infections
EP2968348A4 (en) 2013-03-12 2016-11-09 Curegenix Inc Compounds for treatment of cancer
GB201309180D0 (en) 2013-05-21 2013-07-03 Ucl Business Plc Compounds and Their Uses
WO2015073804A2 (en) 2013-11-15 2015-05-21 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Method of blocking transmission of malarial parasite
EP3077393A1 (en) * 2013-12-06 2016-10-12 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of atr kinase
NO2714752T3 (en) * 2014-05-08 2018-04-21
GB201409044D0 (en) 2014-05-21 2014-07-02 Ucl Business Plc New compounds
EP3560924B1 (en) 2015-04-02 2021-03-31 Merck Patent GmbH Imidazolonyl quinolines and their use as atm kinase inhibitors
CN104876912B (en) 2015-04-08 2017-07-21 苏州云轩医药科技有限公司 Wnt signal path inhibitor and its application
US10858316B2 (en) 2015-07-10 2020-12-08 University Of Maryland, Baltimore Small molecule inhibitors of the MCL-1 oncoprotein and uses thereof
GB201516504D0 (en) * 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
MX2018011105A (en) 2016-03-16 2018-11-22 Kura Oncology Inc Substituted inhibitors of menin-mll and methods of use.

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BR112018004325B1 (en) 2023-10-17
JP6605130B2 (en) 2019-11-13
AU2016323399A1 (en) 2018-05-10
HK1257413A1 (en) 2019-10-18
AU2016323399B2 (en) 2019-04-18
EA033284B1 (en) 2019-09-30
SV2018005655A (en) 2018-04-27
HRP20210149T1 (en) 2021-03-19
HUE053066T2 (en) 2021-06-28
WO2017046216A1 (en) 2017-03-23
NI201800033A (en) 2018-10-18
CN108137576A (en) 2018-06-08
TWI762109B (en) 2022-04-21
EP3350180B1 (en) 2020-11-11
TW202124381A (en) 2021-07-01
US9856255B2 (en) 2018-01-02
SI3350180T1 (en) 2021-03-31
CO2018002829A2 (en) 2018-05-31
CN108137576B (en) 2020-09-22
CA2997399C (en) 2024-02-20
MX2018003186A (en) 2018-05-17
EP3683220A1 (en) 2020-07-22
US11613539B2 (en) 2023-03-28
CR20180172A (en) 2018-05-25
TW201722946A (en) 2017-07-01
IL257847A (en) 2018-04-30
US20210147416A1 (en) 2021-05-20
PH12018500532A1 (en) 2018-08-29
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